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NCT00580788 · FLOW

Participant flow

One Week Parathyroid Hormone-related Protein (PTHrP) IV Dose Escalation Study · Source last updated 2016-02-11

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

groups
  1. description
    PTHrP(1-36) 2 picomoles/kg/hr
    id
    FG000
    title
    Group 1
  2. description
    PTHrP(1-36) 4 picomoles/kg/hr
    id
    FG001
    title
    Group 2
  3. description
    PTHrP (1-36) 5 pmol/kg/hr
    id
    FG002
    title
    Group 3
  4. description
    PTHrP (1-36) 6 picomoles/kg/hr
    id
    FG003
    title
    Group 4
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        1
      type
      Adverse Event
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        6
      3. group Id
        FG002
        num Subjects
        3
      4. group Id
        FG003
        num Subjects
        2
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        6
      3. group Id
        FG002
        num Subjects
        3
      4. comment
        One subject was stopped early for hypertension. One subject completed but was not analyzed.
        group Id
        FG003
        num Subjects
        1
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        1
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
24 subjects were screened and 14 were randomized in the study. Data from 2 subjects was not included in the analysis as there were not enough subjects in that group for analysis. 12 subjects were analyzed.
Complete source fields
groups
  1. description
    PTHrP(1-36) 2 picomoles/kg/hr
    id
    FG000
    title
    Group 1
  2. description
    PTHrP(1-36) 4 picomoles/kg/hr
    id
    FG001
    title
    Group 2
  3. description
    PTHrP (1-36) 5 pmol/kg/hr
    id
    FG002
    title
    Group 3
  4. description
    PTHrP (1-36) 6 picomoles/kg/hr
    id
    FG003
    title
    Group 4
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        1
      type
      Adverse Event
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        6
      3. group Id
        FG002
        num Subjects
        3
      4. group Id
        FG003
        num Subjects
        2
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        6
      3. group Id
        FG002
        num Subjects
        3
      4. comment
        One subject was stopped early for hypertension. One subject completed but was not analyzed.
        group Id
        FG003
        num Subjects
        1
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        1
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
24 subjects were screened and 14 were randomized in the study. Data from 2 subjects was not included in the analysis as there were not enough subjects in that group for analysis. 12 subjects were analyzed.

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice